16 publicaciones de empleo destacadas de staff data en b (¡Están contratando!)

Specimen Receipt and Proc Assoc
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Principal Auditor, QA *GCP Exp Required
Syneos - Clinical and Corporate - Prod —Buenos Aires, Buenos Aires
- Tiempo completo
10d
Sales Enablement and Marketing Operations Specialist
Syneos Health Commercial Solutions —Buenos Aires, Buenos Aires
Piping Engineer
AtkinsRéalis —Buenos Aires, Buenos Aires
- Tiempo completo
Regional Clinical Trial Manager
Boehringer Ingelheim S.A. —Buenos Aires, Buenos Aires
- Tiempo completo
Principal Auditor, QA *GCP Exp Required
サイネオス・ヘルス —Buenos Aires, Buenos Aires
10d
Sr Analyst, Commercial Planning
The Walt Disney Company (LATAM) —Buenos Aires, Buenos Aires
1d
S&P Senior Analyst
DiDi Global —Buenos Aires, Buenos Aires
8d
Sr. CRA (Unblinded)
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
3d
Senior Salesforce Developer
Launchpad Technologies —Capital Federal, Buenos Aires
Postulación rápida
Manager, Commercial Performance & Planning
The Walt Disney Company (LATAM) —Buenos Aires, Buenos Aires
1d
Sr. Safety Specialist
サイネオス・ヘルス —Buenos Aires, Buenos Aires
11d
Senior, Java Software Engineer
Disney Entertainment and ESPN Product & Technology —Buenos Aires, Buenos Aires
Lead C# Software Architect
Marvik —Buenos Aires, Buenos Aires
Senior Clinical Research Associate (Argentina)
Precision Medicine Group —Capital Federal, Buenos Aires
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Florida, Buenos Aires
Postulación rápida

More jobs to discover

Find similar jobs that you might be interested in.

Principal Auditor, QA *GCP Exp Required
Syneos - Clinical and Corporate - Prod —Buenos Aires, Buenos Aires
A minimum 5 years experience within GCP (Phase I-IV Clinical Trials) required. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs,…
10d
Principal Auditor, QA *GCP Exp Required
サイネオス・ヘルス —Buenos Aires, Buenos Aires
A minimum 5 years experience within GCP (Phase I-IV Clinical Trials) required. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs,…
10d

Quiero recibir la alerta de empleo más reciente para staff data en b

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Explorar empleos en más ubicaciones

staff data jobs near b

Empleos de Business Intelligence Analyst en Buenos Aires, Buenos Aires

Empleos de Senior Analyst en Buenos Aires, Buenos Aires

Empleos de Ejecutivo A Comercial Senior en Buenos Aires, Buenos Aires

Empleos de Clinical Data Manager en Buenos Aires, Buenos Aires

Empleos de Intelligence Specialist en Buenos Aires, Buenos Aires

Empleos de Language Specialist en Desde Casa

Empleos de Analista Contable Senior en Capital Federal, Buenos Aires

Empleos de Operations Specialist Ecommerce en Provincia De Buenos Aires

Empleos de Desarrollador A Senior en Córdoba, Córdoba

Empleos de Senior Project Manager en Buenos Aires, Buenos Aires

Empleos de Research Analyst en Buenos Aires, Buenos Aires

Empleos de Unity Developer en Buenos Aires, Buenos Aires

Empleos de Backend Developer en Capital Federal, Buenos Aires

Empleos de Fullstack Developer en Remote

Empleos de Trainee, Developer en Canning, Buenos Aires

Empleos de Ingeniero A De Software en Buenos Aires, Buenos Aires

Empleos de Desarrollador A De Software en Buenos Aires, Buenos Aires

Empleos de Finance Controlling Analyst en Buenos Aires, Buenos Aires

Empleos de Financial Analyst en Buenos Aires, Buenos Aires

Empleos de Systems Analyst en Provincia De Buenos Aires

Specimen Receipt and Proc Assoc

IQVIA -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Office-based | R1552337

Job Overview

The Specimen Receipt and Processing Associate is responsible for assisting with a variety of routine activities associated with receipt of clinical specimens.

Essential Functions

Responsible for assisting with receipt of consignments and shipments

Responsible for the opening of shipments and the quality check of patient info forms. Escalates incorrect,missing information, or damaged shipments to senior level staff

Responsible for correct disposal and/or recycling of kit shipping supplies

Ensures specimens are not left in kit packaging by conducting a secondary check of shipping materials.

Supports and responds to after-hour alarms and/or other job critical functions.

Assists in maintenance of equipment.

Assists with supply inventory functions and general clean up of workstations.

Performs various administrative duties as required.

Responsible for organizing the work area, as requested by management.

Dependent upon functional area, may also handle receipt of compounds and control material.

Responsible for following safety procedures.

Participates in continuing education through self study and attendance of meetings.

Performs work in accordance with company procedures and applicable regulatory guidelines.

Qualifications

High School Diploma or equivalent

Basic Computer skills.

Ability to maintain effective reporting procedures and control workflow.

Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Please note that this role requires on-site work from Tuesday to Saturday. Working hours to be confirmed.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Postulate ahora

Refiná tu búsqueda

staff data empleos en b

Specimen Receipt and Proc Assoc

Principal Auditor, QA *GCP Exp Required

Sales Enablement and Marketing Operations Specialist

Piping Engineer

Regional Clinical Trial Manager

Principal Auditor, QA *GCP Exp Required

Sr Analyst, Commercial Planning

S&P Senior Analyst

Sr. CRA (Unblinded)

Senior Salesforce Developer

Manager, Commercial Performance & Planning

Sr. Safety Specialist

Senior, Java Software Engineer

Lead C# Software Architect

Senior Clinical Research Associate (Argentina)

Senior Clinical Research Associate (level dependent on experience)

More jobs to discover

Quiero recibir la alerta de empleo más reciente para staff data en b

Related Searches

Explorar empleos en más ubicaciones

Where you'll work

Office-based

Culture

Herramientas para candidatos

Herramientas para empresas

Explorar

Mantente conectado